A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14955199



Internal ID3930520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31894408..31910209hg38UCSC Ensembl
Innerchr14:31894908..31909709hg38UCSC Ensembl
Outerchr14:31893408..31911209hg38UCSC Ensembl
chr14:32363614..32379415hg19UCSC Ensembl
Innerchr14:32364114..32378915hg19UCSC Ensembl
Outerchr14:32362614..32380415hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3815802
hg1915802
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633979
Supporting Variants
SamplesHG03583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14955199
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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